Helicobacter pylori multiplex serology and risk of non-cardia and cardia gastric cancer: a case-cohort study and meta-analysis

Author:

Yao Pang1,Kartsonaki Christiana12,Butt Julia3ORCID,Jeske Rima3,de Martel Catherine4,Plummer Martyn5,Guo Yu6,Clark Sarah12,Walters Robin G12,Chen Yiping12,Avery Daniel1,Lv Jun78,Yu Canqing78ORCID,Wang Hao9,Hill Michael12ORCID,Peto Richard1,Li Liming78,Waterboer Tim3,Chen Zhengming12,Millwood Iona Y12,Yang Ling12

Affiliation:

1. Clinical Trial Service Unit & Epidemiological Studies Unit (CTSU), Nuffield Department of Population Health, University of Oxford , Oxford, UK

2. Medical Research Council Population Health Research Unit (MRC PHRU), Nuffield Department of Population Health, University of Oxford , Oxford, UK

3. Infections and Cancer Epidemiology Division, German Cancer Research Center (DKFZ) , Heidelberg, Germany

4. Early Detection, Prevention and Infections Branch, International Agency for Research on Cancer , Lyon, France

5. Department of Statistics, University of Warwick , Coventry, UK

6. National Center for Cardiovascular Diseases, Fuwai Hospital, Chinese Academy of Medical Sciences , Beijing, China

7. Department of Epidemiology and Biostatistics, School of Public Health, Peking University , Beijing, China

8. Center for Public Health and Epidemic Preparedness & Response, Peking University , Beijing, China

9. NCDs Prevention and Control Department, Zhejiang CDC , Zhejiang, China

Abstract

Abstract Background Helicobacter pylori infection is a major cause of non-cardia gastric cancer (NCGC), but uncertainty remains about the associations between sero-positivity to different H. pylori antigens and risk of NCGC and cardia gastric cancer (CGC) in different populations. Methods A case-cohort study in China included ∼500 each of incident NCGC and CGC cases and ∼2000 subcohort participants. Sero-positivity to 12 H. pylori antigens was measured in baseline plasma samples using a multiplex assay. Hazard ratios (HRs) of NCGC and CGC for each marker were estimated using Cox regression. These were further meta-analysed with studies using same assay. Results In the subcohort, sero-positivity for 12 H. pylori antigens varied from 11.4% (HpaA) to 70.8% (CagA). Overall, 10 antigens showed significant associations with risk of NCGC (adjusted HRs: 1.33 to 4.15), and four antigens with CGC (HRs: 1.50 to 2.34). After simultaneous adjustment for other antigens, positive associations remained significant for NCGC (CagA, HP1564, HP0305) and CGC (CagA, HP1564, HyuA). Compared with CagA sero-positive only individuals, those who were positive for all three antigens had an adjusted HR of 5.59 (95% CI 4.68–6.66) for NCGC and 2.17 (95% CI 1.54–3.05) for CGC. In the meta-analysis of NCGC, the pooled relative risk for CagA was 2.96 (95% CI 2.58–3.41) [Europeans: 5.32 (95% CI 4.05–6.99); Asians: 2.41 (95% CI 2.05–2.83); Pheterogeneity<0.0001]. Similar pronounced population differences were also evident for GroEL, HP1564, HcpC and HP0305. In meta-analyses of CGC, two antigens (CagA, HP1564) were significantly associated with a higher risk in Asians but not Europeans. Conclusions Sero-positivity to several H. pylori antigens was significantly associated with an increased risk of NCGC and CGC, with varying effects between Asian and European populations.

Funder

CRUK PRC-Project Award

China Kadoorie Biobank

Kadoorie Charitable Foundation

Wellcome Trust

National Natural Science Foundation of China

National Key Research and Development Program of China

Medical Research Council

Cancer Research UK

British Heart Foundation

Publisher

Oxford University Press (OUP)

Subject

General Medicine,Epidemiology

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